nucleotides and nucleic acids Flashcards

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1
Q

nucleotides

A

DNA and RNA are nucleic acids: polymers that are made up of many repeating units (monomers) called nucleotides
Each nucleotide is formed from:
A pentose sugar (a sugar with 5 carbon atoms)
A nitrogen-containing organic base
A phosphate group

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2
Q

dna nucleotides

A

The components of a DNA nucleotide are:
A deoxyribose sugar with hydrogen at the 2’ position
A phosphate group
One of four nitrogenous bases - adenine (A), cytosine(C), guanine(G) or thymine(T)

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3
Q

rna nucleotides

A

The components of an RNA nucleotide are:
A ribose sugar with a hydroxyl (OH) group at the 2’ position
A phosphate group
One of four nitrogenous bases - adenine (A), cytosine(C), guanine(G) or uracil (U)
The presence of the 2’ hydroxyl group makes RNA more susceptible to hydrolysis
This is why DNA is the storage molecule and RNA is the transport molecule with a shorter molecular lifespan

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4
Q

purines and pyrimidines

A

The nitrogenous base molecules that are found in the nucleotides of DNA (A, T, C, G) and RNA (A, U, C, G) occur in two structural forms: purines and pyrimidines
The bases adenine and guanine are purines – they have a double ring structure
The bases cytosine, thymine and uracil are pyrimidines – they have a single ring structure

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5
Q

phosphodiester bond

A

DNA and RNA are polymers (polynucleotides), meaning that they are made up of many nucleotides joined together in long chains
Separate nucleotides are joined together via condensation reactions
These condensation reactions occur between the phosphate group of one nucleotide and the pentose sugar of the next nucleotide
A condensation reaction between two nucleotides forms a phosphodiester bond
It is called a phosphodiester bond because it consists of a phosphate group and two ester bonds
The chain of alternating phosphate groups and pentose sugars produced as a result of many phosphodiester bonds is known as the sugar-phosphate backbone (of the DNA or RNA molecule)
As the synthesis of polynucleotides requires the formation of phosphodiester bonds, the same is true for the reverse process: the breakdown of polynucleotides requires the breakage of phosphodiester bonds

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6
Q

structure of atp and add

A

All organisms require a constant supply of energy to maintain their cells and stay alive

In all organisms this energy is required for:
Anabolic reactions (building larger molecules from smaller molecules)
Moving substances across the cell membrane or moving substances within the cell
In animals energy is also required for:
Muscle contraction – to coordinate movement at the whole-organism level
The conduction of nerve impulses

In all known forms of life, ATP from respiration is used to transfer energy in all energy-requiring processes in cells
This is why ATP is known as the universal energy currency
Adenosine Triphosphate (ATP) is a nucleotide
The monomers of DNA and RNA are also nucleotide

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7
Q

atp

A

Adenosine triphosphate (ATP) is the energy-carrying molecule that provides the energy to drive many processes inside living cells

ATP is another type of nucleic acid and hence it is structurally very similar to the nucleotides that make up DNA and RNA

It is a phosphorylated nucleotide
Adenosine (a nucleoside) can be combined with one, two or three phosphate groups
One phosphate group = adenosine monophosphate (AMP)
Two phosphate groups = adenosine diphosphate (ADP)
Three phosphate groups = adenosine triphosphate (ATP)

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8
Q

dna structure

A

The nucleic acid DNA is a polynucleotide – it is made up of many nucleotides bonded together in a long chain

DNA molecules are made up of two polynucleotide strands lying side by side, running in opposite directions – the strands are said to be antiparallel

Each DNA polynucleotide strand is made up of alternating deoxyribose sugars and phosphate groups bonded together to form the sugar-phosphate backbone. These bonds are covalent bonds known as phosphodiester bonds

The phosphodiester bonds link the 5-carbon of one deoxyribose sugar molecule to the phosphate group from the same nucleotide, which is itself linked by another phosphodiester bond to the 3-carbon of the deoxyribose sugar molecule of the next nucleotide in the strand
Each DNA polynucleotide strand is said to have a 3’ end and a 5’ end (these numbers relate to which carbon on the pentose sugar could be bonded with another nucleotide)
As the strands run in opposite directions (they are antiparallel), one is known as the 5’ to 3’ strand and the other is known as the 3’ to 5’ strand

The nitrogenous bases of each nucleotide project out from the backbone towards the interior of the double-stranded DNA molecule

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9
Q

hydrogen bonding

A

The two antiparallel DNA polynucleotide strands that make up the DNA molecule are held together by hydrogen bonds between the nitrogenous bases

These hydrogen bonds always occur between the same pairs of bases:
The purine adenine (A) always pairs with the pyrimidine thymine (T) – two hydrogen bonds are formed between these bases
The purine guanine (G) always pairs with the pyrimidine cytosine (C) – three hydrogen bonds are formed between these bases

This is process is known as complementary base pairing and the pairs are known as complementary base pairs

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10
Q

double helix

A

DNA is not two-dimensional as seen in the diagram above
DNA is described as a double helix (this refers to the three-dimensional shape formed by the twisting of the DNA molecule)

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11
Q

semi-conservative replication of DNA

A

Before a (parent) cell divides, it needs to copy the DNA contained within it
Doubling the DNA ensures that the two new (daughter) cells produced will both receive full copies of the parental DNA
The DNA is copied via a process known as semi-conservative replication (semi = half)
The process is called this because in each new DNA molecule produced, one of the polynucleotide DNA strands (half of the new DNA molecule) is from the original DNA molecule being copied
The other polynucleotide DNA strand (the other half of the new DNA molecule) has to be newly created by the cell
Therefore, the new DNA molecule has conserved half of the original DNA and then used this to create a new strand

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12
Q

the importance of retaining one original DNA strand

A

Retaining one original DNA strand ensures there is genetic continuity (i.e. genetic information is conserved) between generations of cells

In other words, it ensures that the new cells produced during cell division inherit all their genes from their parent cells

This is important because cells in our body are replaced regularly and therefore we need the new cells to be able to do the same role as the old ones
Replication of DNA and cell division also occurs during growth

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13
Q

semi conservative replication

A

DNA replication occurs in preparation for mitosis, when a parent cell divides to produce two genetically identical daughter cells – as each daughter cell contains the same number of chromosomes as the parent cell, the number of DNA molecules in the parent cell must be doubled before mitosis takes place

DNA replication occurs during the S phase of the cell cycle (which occurs during interphase, when a cell is not dividing)

The enzyme helicase unwinds the DNA double helix by breaking the hydrogen bonds between the base pairs on the two antiparallel polynucleotide DNA strands to form two single polynucleotide DNA strands

Each of these single polynucleotide DNA strands acts as a template for the formation of a new strand made from free nucleotides that are attracted to the exposed DNA bases by base pairing

The new nucleotides are then joined together by the enzyme DNA polymerase which catalyses condensation reactions to form a new strand

The original strand and the new strand join together through hydrogen bonding between base pairs to form the new DNA molecule
This method of replicating DNA is known as semi-conservative replication because half of the original DNA molecule is kept (conserved) in each of the two new DNA molecules

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14
Q

dna polymerase

A

In the nucleus, there are free nucleotides which contain three phosphate groups
These nucleotides are known as nucleoside triphosphates or ‘activated nucleotides’

The extra phosphates activate the nucleotides, enabling them to take part in DNA replication
The bases of the free nucleoside triphosphates align with their complementary bases on each of the template DNA strands

The enzyme DNA polymerase synthesises new DNA strands from the two template strands
It does this by catalysing condensation reactions between the deoxyribose sugar and phosphate groups of adjacent nucleotides within the new strands, creating the sugar-phosphate backbone of the new DNA strands

DNA polymerase cleaves (breaks off) the two extra phosphates and uses the energy released to create the phosphodiester bonds (between adjacent nucleotides)
Hydrogen bonds then form between the complementary base pairs of the template and new DNA strands

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15
Q

mutations

A

The replicated DNA molecules must be an exact copy of the parent DNA molecule, therefore the formation of the complementary strands must be a highly accurate process

Although the process is astonishingly accurate considering it is happening constantly in cells and at a considerable speed, occasional mistakes occur in the form of:
Bases being inserted into the complementary strand in the wrong order
An extra base being inserted by accident
A base being left out by accident

These mistakes in the process of semi-conservative replication of DNA result in the occurrence of random, spontaneous mutations (i.e. errors in the genetic code)

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16
Q

nature of the genetic code

A

A gene is a sequence of nucleotides that forms part of a DNA molecule (one DNA molecule contains many genes)

This sequence of nucleotides (the gene) codes for the production of a specific polypeptide (protein)

Protein molecules are made up of a series of amino acids bonded together
The shape and behaviour of a protein molecule depends on the exact sequence of these amino acids (the initial sequence of amino acids is known as the primary structure of the protein molecule)

The genes in DNA molecules, therefore, control protein structure (and as a result, protein function) as they determine the exact sequence in which the amino acids join together when proteins are synthesised in a cell

17
Q

the triplet code

A

The sequence of DNA nucleotide bases found within a gene is determined by a triplet (three-letter) code

Each sequence of three bases (i.e. each triplet of bases) in a gene codes for one amino acid
These triplets codes for different amino acids – there are 20 different amino acids that cells use to make up different proteins
For example:
CAG codes for the amino acid valine
TTC codes for the amino acid lysine
GAC codes for the amino acid leucine
CCG codes for the amino acid glycine

Some of these triplets of bases code for start (TAC – methionine) and stop signals
These start and stop signals tell the cell where individual genes start and stop

As a result, the cell reads the DNA correctly and produces the correct sequences of amino acids (and therefore the correct protein molecules) that it requires to function properly
The genetic code is non-overlapping
Each base is only read once in which codon it is part of

18
Q

genetic code

A

There are four bases, so there are 64 different codons (triplets) possible (43 = 64), yet there are only 20 amino acids that commonly occur in biological proteins

This is why the code is said to be degenerate: multiple codons can code for the same amino acids
The degenerate nature of the genetic code can limit the effect of mutations
The genetic code is also universal, meaning that almost every organism uses the same code (there are a few rare and minor exceptions)

The same triplet codes code for the same amino acids in all living things (meaning that genetic information is transferable between species)
The universal nature of the genetic code is why genetic engineering (the transfer of genes from one species to another) is possible

19
Q

codons and anticodons

A

Once mRNA has been formed and left the nucleus it moves to the ribosomes where it can as a template for protein synthesis
Each triplet within the mRNA code is described as a codon
The tRNA molecules that transfer amino acids possess anticodons which are complementary to the codons on mRNA

20
Q

protein synthesis stages

A

A gene is a sequence of nucleotide bases in a DNA molecule that codes for the production of a specific sequence of amino acids, that in turn make up a specific polypeptide (protein)
This process of protein synthesis occurs in two stages:
Transcription – DNA is transcribed and an mRNA molecule is produced
Translation – mRNA (messenger RNA) is translated and an amino acid sequence is produced

21
Q

transcription

A

This stage of protein synthesis occurs in the nucleus of the cell
Part of a DNA molecule unwinds (the hydrogen bonds between the complementary base pairs break)
The exposed gene can then be transcribed (the gene from which a particular polypeptide will be produced)
A complimentary copy of the code from the gene is made by building a single-stranded nucleic acid molecule known as mRNA (messenger RNA)
Free RNA nucleotides pair up (via hydrogen bonds) with their complementary (now exposed) bases on one strand (the template strand) of the ‘unzipped’ DNA molecule
The sugar-phosphate groups of these RNA nucleotides are then bonded together (by phosphodiester bonds) by the enzyme RNA polymerase to form the sugar-phosphate backbone of the mRNA molecule
When the gene has been transcribed (when the mRNA molecule is complete), the hydrogen bonds between the mRNA and DNA strands break and the double-stranded DNA molecule re-forms
The mRNA molecule then leaves the nucleus via a pore in the nuclear envelope

22
Q

the coding strand and the template strand

A

In the transcription stage of protein synthesis, free RNA nucleotides pair up with the exposed bases on the DNA molecule

RNA nucleotides only pair with the bases on one strand of the DNA molecule
This strand of the DNA molecule is known as the template strand (or the transcribed strand) and it is used to produce the mRNA molecule

The other strand is known as the coding strand (or the non-template or non-transcribed strand)
RNA polymerase moves along the template strand in the 3’ to 5’ direction
This means that the mRNA molecule grows in the 5’ to 3’ direction

Because the mRNA is formed by complementary pairing with the DNA template strand, the mRNA molecule contains the exact same sequence of nucleotides as the DNA coding strand (although the mRNA will contain uracil instead of thymine)

23
Q

translation

A

Translation occurs in the cytoplasm of the cell
After leaving the nucleus via a nuclear pore, the mRNA molecule attaches to a ribosome
In the cytoplasm, there are free molecules of tRNA (transfer RNA)

These tRNA molecules have a triplet of unpaired bases at one end (known as the anticodon) and a region where a specific amino acid can attach at the other

There are about 20 different tRNA molecules, each with a specific anticodon and specific amino acid binding site
The tRNA molecules bind with their specific amino acids (also in the cytoplasm) and bring them to the mRNA molecule on the ribosome

The triplet of bases (anticodon) on each tRNA molecule pairs with a complementary triplet (codon) on the mRNA molecule

Two tRNA molecules fit onto the ribosome at any one time, bringing the amino acid they are each carrying side by side
A peptide bond is then formed (via a condensation reaction) between the two amino acids

This process continues until a ‘stop’ codon on the mRNA molecule is reached – this acts as a signal for translation to stop and at this point the amino acid chain coded for by the mRNA molecule is complete
The amino acid chain then forms the final polypeptide